RGD:150331924 Rat Genome Database

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Variant: RGD:150331924 -  Homo sapiens

RGD ID: 150331924
RS ID: rs141985285
ClinVar ID: CV1171578
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105375056  TREM2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 41,126,910
GRCh38 6 41,159,172
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018965.4:c.483-106G>A
NM_001271821.2:c.483-392G>A
LRG_631:g.9013G>A
NG_011561.1:g.9013G>A
More... 		08/23/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TREM2
Accession:NM_018965
Location:INTRON

Gene Symbol:TREM2
Accession:NM_001271821
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001538833 CLINVAR
dbSNP (RS) rs141985285 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TREM2 CLINVAR
OMIM 605086 CLINVAR